19-Oxo-PGF2 analogs

ABSTRACT

The present invention provides novel 19-oxo-PGF 2  analogs, which are useful for a variety of pharmacological purposes, e.g., antiasthmatic indications.

DESCRIPTION CROSS REFERENCE TO RELATED APPLICATION

This application is a division of Ser. No. 025,879, filed Apr. 2, 1979, now pending.

BACKGROUND OF THE INVENTION

The present invention relates to novel prostaglandin analogs. Particularly, the invention relates to prostaglandin analogs wherein the C-19 position is substituted by oxo, i.e., 19-keto-PG compounds or 19-oxo-PG compounds. Most particularly, the present invention relates to novel 19-Oxo-PGF₂ analogs, a disclosure of the preparation and pharmacological use of which is incorporated here by reference from U.S. Pat. No. 4,228,104.

PRIOR ART

Prostaglandins exhibiting a variety of substitution at the C-19 position are known. See particularly J. C. Sih, et al., JACS 91:3685 (1969) wherein 19-oxo-PGE₂ and 13,14-dihydro-19-oxo-PGE₁ are disclosed. Further, Chemical Abstracts 86:43265H purportedly discloses 19-oxo-PGF₂ α. The abstract is derived from Japanese Kokai No. 76 82,245.

SUMMARY OF THE INVENTION

The present invention particularly provides:

a compound of the formula ##STR1## wherein D is

(1) cis--CH═CH--CH₂ --(CH₂)_(g) --CH₂ --,

(2) cis--CH═CH--CH₂ --(CH₂)_(g) --CF₂ --,

(3) cis--CH₂ --CH═CH--CH₂ --CH₂ --, or

(4) trans--(CH₂)₃ --CH═CH--;

wherein g is zero, one, two, or three; wherein Q is α--OH:β--R₅ or α--R₅ :β--OH, wherein R₅ is hydrogen or methyl; wherein R₆ is

(a) hydrogen,

(b) alkyl of one to 12 carbon atoms, inclusive,

(c) cycloalkyl of 3 to 10 carbon atoms, inclusive,

(d) aralkyl of 7 to 12 carbon atoms, inclusive,

(e) phenyl,

(f) phenyl substituted with one, 2, or 3 chloro or alkyl groups of one to 3 carbon atoms, inclusive,

(g) -(p--Ph)--CO--CH₃,

(h) -(p--Ph)--NH--CO--(p--Ph)--NH--CO--CH₃,

(i) -(p--Ph)--NH--CO--(p--Ph),

(j) -(p--Ph)--NH--CO--CH₃,

(k) -(p--Ph)--NH--CO--NH₂,

(l) -(p--Ph)--CH═N--NH--CO--NH₂,

(m) β-naphthyl,

(n) --CH₂ --CO--R₂₈, wherein (p--Ph) is para-phenyl or inter-para-phenylene, wherein R₂₈ is phenyl, p-bromophenyl, p-biphenylyl, p-nitrophenyl, p-benzamidophenyl, or 2-naphthyl, or

(o) a pharmacologically acceptable cation;

wherein R₃ and R₄ are hydrogen, methyl, or fluoro, being the same or different, with the proviso that one of R₃ and R₄ is fluoro only when the other is hydrogen or fluoro; and wherein X is cis-- or trans--CH═CH--; with the proviso that R₆ is not hydrogen or alkyl of one to 12 carbon atoms, inclusive, when Q is α--OH:β--H, R₂ is hydroxy, R₃ and R₄ are hydrogen or methyl and D is cis--CH═CH--CH₂ --(CH₂)_(g) --CH₂ --.

The compounds of the present invention are particularly useful for inducing prostaglandin-like biological effects, as described in U.S. Ser. No. 026,066. Uses of compounds in accordance with the present invention include, therefore, antiasthmatic indications.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention particularly relates to:

16,16-Difluoro-19-oxo-PGE₂ ; and

16,16-Difluoro-(15R)-19-oxo-PGE₂. 

I claim:
 1. A compound of the formula ##STR2## wherein D is cis--CH═CH--CH₂ --(CH₂)_(g) --CH₂ --;wherein g is zero, one, two, or three; wherein Q is α--OH:β--R₅ or α--R₅ :β--OH, wherein R₅ is hydrogen or methyl; wherein R₆ is (a) hydrogen, (b) alkyl of one to 12 carbon atoms, inclusive, (c) cycloalkyl of 3 to 10 carbon atoms, inclusive, (d) aralkyl of 7 to 12 carbon atoms, inclusive, (e) phenyl, (f) phenyl substituted with one, 2, or 3 chloro or alkyl groups of one to 3 carbon atoms, inclusive, (g) -(p--Ph)--CO--CH₃, (h) -(p--Ph)--NH--CO--(p--Ph)--NH--CO--CH₃, (i) -(p--Ph)--NH--CO--(p--Ph), (j) -(p--Ph)--NH--CO--CH₃, (k) -(p--Ph)--NH--CO--NH₂, (l) -(p--Ph)--CH═N--NH--CO--NH₂, (m) β-naphthyl, (n) --CH₂ --CO--R₂₈,wherein (p--Ph) is para-phenyl or inter-para-phenylene, wherein R₂₈ is phenyl, p-bromophenyl, p-biphenylyl, p-nitrophenyl, p-benzamidophenyl, or 2-naphthyl, or (o) a pharmacologically acceptable cation;wherein R₃ and R₄ are hydrogen, methyl, or fluoro, being the same or different, with the proviso that one of R₃ and R₄ is fluoro only when the other is hydrogen or fluoro; and wherein X is cis-- or trans--CH═CH--; with the proviso that R₆ is not hydrogen or alkyl of one to 12 carbon atoms, inclusive, when Q is α--OH:β--H, R₂ is hydroxy, R₃ and R₄ are hydrogen or methyl and D is cis--CH═CH--CH₂ --(CH₂)_(g) --CH₂ --.
 2. A compound according to claim 1, wherein R₆ is hydrogen or methyl.
 3. 16,16-Difluoro-19-oxo-PGE₂, an analog according to claim
 2. 4. 16,16-Difluoro-15(R)-19-Oxo-PGE₂, an analog according to claim
 2. 